Canonical Allele Identifier: CA369653633

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048790C>G (hg19) ; chr7:g.143351697C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351697C>G , CM000669.2:g.143351697C>G	GRCh38
NC_000007.13:g.143048790C>G , CM000669.1:g.143048790C>G	GRCh37
NC_000007.12:g.142758912C>G	NCBI36
NG_009815.1:g.40572C>G
NG_009815.2:g.40572C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2699C>G	ENSP00000498052.2:p.Pro900Arg
ENST00000343257.7:c.2699C>G MANE Select	ENSP00000339867.2:p.Pro900Arg
ENST00000432192.6:c.2523C>G
ENST00000343257.6:c.2699C>G	ENSP00000339867.2:p.Pro900Arg
NM_000083.2:c.2699C>G	NP_000074.2:p.Pro900Arg
NR_046453.1:n.2639C>G
XM_011515781.1:c.2723C>G	XP_011514083.1:p.Pro908Arg
XM_011515782.1:c.1445C>G	XP_011514084.1:p.Pro482Arg
XM_011515782.2:c.1445C>G	XP_011514084.1:p.Pro482Arg
XM_017011739.1:c.2273C>G	XP_016867228.1:p.Pro758Arg
XM_017011740.1:c.2249C>G	XP_016867229.1:p.Pro750Arg
NM_000083.3:c.2699C>G MANE Select	NP_000074.3:p.Pro900Arg
NR_046453.2:n.2654C>G